BDBM50326162 8-[2-(3-Iodophenyl)thiazol-4-yl]dibenzo[b,d]furan-4-carboxylic acid::CHEMBL1242826

SMILES OC(=O)c1cccc2c3cc(ccc3oc12)-c1csc(n1)-c1cccc(I)c1

InChI Key InChIKey=DSFHVHHMKNFHKR-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50326162   

TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50326162(8-[2-(3-Iodophenyl)thiazol-4-yl]dibenzo[b,d]furan-...)
Affinity DataIC50: 425nMAssay Description:Inhibition of human recombinant PTP1B after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/11/2011
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Human)
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50326162(8-[2-(3-Iodophenyl)thiazol-4-yl]dibenzo[b,d]furan-...)
Affinity DataIC50: 1.62E+3nMAssay Description:Inhibition of human recombinant TCPTP after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/11/2011
Entry Details Article
PubMed
TargetReceptor-type tyrosine-protein phosphatase F(Human)
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50326162(8-[2-(3-Iodophenyl)thiazol-4-yl]dibenzo[b,d]furan-...)
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of human recombinant LAR after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/11/2011
Entry Details Article
PubMed